Neuropsychological Profiles Differ among the Three Variants of Primary Progressive Aphasia

被引:63
|
作者
Butts, Alissa M. [1 ]
Machulda, Mary M. [1 ]
Duffy, Joseph R. [2 ]
Strand, Edythe A. [2 ]
Whitwell, Jennifer L. [3 ]
Josephs, Keith A. [4 ]
机构
[1] Mayo Clin, Dept Psychiat & Psychol Neuropsychol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Neurol Speech Pathol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Radiol, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Neurol Behav Neurol, Rochester, MN 55905 USA
关键词
Primary progressive aphasia; Neuropsychology; Logopenic; Agrammatic; Semantic; Cognition; LONGITUDINAL CHANGES; DEMENTIA; SPEECH; CLASSIFICATION; PATHOLOGY; APRAXIA; NORMS; TOKEN; FORM;
D O I
10.1017/S1355617715000399
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The objective of this study was to describe the neuropsychological profiles of the three variants of primary progressive aphasia (PPA). Based on a comprehensive speech and language evaluation, 91 subjects were classified as logopenic (lvPPA = 51), semantic (svPPA = 13), or agrammatic (agPPA = 27). All subjects completed a separate neuropsychological evaluation assessing verbal and visual memory, processing speed, executive function, and visuospatial function. The groups did not differ on demographic variables or on measures of disease duration or aphasia severity. There were group differences on aspects of learning and memory, as well as aspects of executive and visuospatial functions, primarily with the lvPPA group performing lower than the agPPA and svPPA groups. The agPPA group showed subtle deficits consistent with frontal lobe impairment, whereas neurocognitive weaknesses in the svPPA group were restricted to temporal lobe functions. The pattern of neurocognitive dysfunction in lvPPA suggests disease involvement of frontal lobe functions in addition to temporoparietal functions. These neurocognitive findings emphasize the value of a comprehensive neuropsychological evaluation of individuals who present with primary language disturbance, given the pattern of cognitive deficits may provide additive information for differentiating these clinical syndromes.
引用
收藏
页码:429 / 435
页数:7
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